Variant #0000442370 (NC_000003.11:g.183696402A>G, NM_005688.2:c.1185T>C (ABCC5))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.183696402A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC5_000170
Frequency 7717/12448
Freq. EA 4731/8378
Freq. AA 2986/4070
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:23:53 +02:00 (CEST)
Date last edited 2018-08-23 09:50:46 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC5 NM_005688.2 ?/? c.1185T>C r.(=) p.(=)